Manager, Manufacturing

Role: Manufacturing Manager I oversees cell therapy production processes in a cGMP environment, focusing on process execution, technical assessment, and compliance. Responsibilities include managing creation and adherence to Source Governing Documents, supervising daily operations, ensuring a compliant, safe, and inspection-ready manufacturing environment, and leading process troubleshooting and improvement initiatives. The role involves team leadership, training, performance evaluation, and fostering a culture of safety, quality, and continuous improvement. Qualifications: Bachelor's in science or engineering, with 5+ years in cGMP cell therapy or bioprocessing manufacturing, including 2+ years of leadership experience. Preferred experience in aseptic processing, bioreactor operations, cell separation, and cryopreservation. The role requires working in cleanroom environments, handling human-derived materials, and operating in BSL2/ML-1 settings, with shift flexibility including days, swing, or nights. High-value specifics include cell therapy modalities, BSL2 handling, and process validation. Reporting to Sr. Manager or Associate Director, with no explicit mention of cross-functional interactions. Location: Bothell, WA, US; work involves standing, gowning, lifting, and working in controlled environments.